Composition for stabilizing chlorine dioxide

ABSTRACT

A composition for stabilizing chlorine dioxide maintains a chlorine dioxide concentration nearly constant in the agent containing chlorine dioxide dissolved therein even when chlorine dioxide is continuously released as gas from agent, and includes a chlorite and a pH adjuster. The pH adjuster is an acid or a salt thereof having a buffering property whose pH is 2.5 to 6.8 as a 5% aqueous solution at 25° C.

TECHNICAL FIELD

The present invention relates to a composition for stabilizing chlorinedioxide (hereinbelow, frequently simply referred to as “stabilizingcomposition”) which can maintain a chlorine dioxide concentrationconstant for a long term in an agent containing chlorine dioxidedissolved therein, that is, which can maintain the chlorine dioxideconcentration nearly constant even when chlorine dioxide is continuouslyreleased by portions as gas from the agent (or even when chlorinedioxide gas is aggressively kept released).

BACKGROUND ART

It is well known that chlorine dioxide gas is a strong oxidant, and itsoxidizing action is effective in sterilization and decomposition ofmalodorous substances. Therefore, chlorine dioxide has been used indisinfectant, deodorant and the like. Chlorine dioxide is dissolved inwater in 20 times its volume of water, to give a brownish yellow aqueoussolution. From the viewpoint of easiness in handling, it is desirable touse chlorine dioxide in a form of such an aqueous solution. However,when the aqueous solution of chlorine dioxide is brought into contactwith air, chlorine dioxide gas is rapidly generated. Therefore, therehas been proposed a technique in which chlorine dioxide gas isconstantly generated while maintaining its stability, by dissolvingchlorine dioxide gas in an aqueous solution of sodium peroxycarbonate,and thus by forming an aqueous solution containing sodium chlorite as amain component at a retained pH of 9, i.e., what is called a stabilizedaqueous solution of chlorine dioxide (see Patent Document 1).

The stabilized aqueous solution of chlorine dioxide is retained at pH 9(alkali) for the purpose of maintaining stability, as described above.Therefore, a generation amount of free chlorine dioxide gas havingdisinfecting and deodorizing effects or the like is extremely low, andthus it is difficult to attain satisfactory disinfecting and deodorizingeffects or the like. Therefore, in order to enhance the activity of thestabilized aqueous solution of chlorine dioxide, an acid has been addedimmediately before its use to lower the pH to 7 or less, for generatingchlorine dioxide gas, to thereby elicit activity.

However, the generation of chlorine dioxide gas is extremely rapid, andchlorine dioxide does not have sustained activity. As a result, therearise economical problems that processes and equipments or facilities toimplement the processes are required in order to activate the chlorinedioxide solution and to continuously generate chlorine dioxide gas. Inaddition, since chlorine dioxide gas is rapidly generated in theconventional stabilized aqueous solution of chlorine dioxide asdescribed above, a chlorine dioxide activity is not retained constantand sometimes reaches an extremely high level, which raises safetyconcern about effects on animals, especially on human being, and thechlorine dioxide has not been used without anxiety.

In order to solve the above-mentioned problems, there has been proposeda technique in which a mixture prepared by adding an organic acid, suchas citric acid, to chlorite is blended with a dissolved chlorine dioxidesolution, to thereby maintain a chlorine dioxide concentration nearlyconstant for a long term (see Patent Document 2).

-   Patent Document 1: Japanese Patent Application JP61-181532A-   Patent Document 2: Japanese Patent JP3110724B

DISCLOSURE OF THE INVENTION

According to the technique disclosed in Patent Document 2, the chlorinedioxide concentration can be maintained constant for a long term withoutrapidly generating gas, and even when chlorine dioxide is continuouslyreleased by portions as gas, the chlorine dioxide concentration can beheld in an approximately constant range. However, the preservationstability is not necessarily satisfactory, and there is a room forimprovement.

The present invention is made with the view toward solving theabove-mentioned problems, and the object is to provide a stabilizingcomposition having excellent preservation stability, in which thechlorine dioxide concentration of the agent containing chlorine dioxidecan be held in an approximately constant range for a long term.

In one aspect of the present invention, a composition for stabilizingchlorine dioxide, which can maintain a chlorine dioxide concentrationnearly constant in an agent containing chlorine dioxide dissolvedtherein even when chlorine dioxide is continuously released as gas fromthe agent, includes a chlorite and a pH adjuster which is an acid or asalt thereof having a buffering property whose pH is 2.5 to 6.8 as a 5%aqueous solution at 25° C.

According to the stabilizing composition of the present invention,excellent preservation stability can be obtained. For example, thechlorine dioxide concentration of the agent containing chlorine dioxidecan be maintained constant for a long term, and even when chlorinedioxide is continuously released by portions as gas from the agent (oreven when chlorine dioxide gas is aggressively kept released), thechlorine dioxide concentration in the agent can be held in anapproximately constant range. The expression “continuously released byportions as gas” herein means that, for example, during transportationor preservation, even though a lid of a container is closed, chlorinedioxide dissipates as gas in the course of nature, and the expression“chlorine dioxide gas is aggressively kept released” herein means thatchlorine dioxide gas is released to a gas phase with an expectation ofobtaining deodorizing and disinfecting action in the gas phase.

Herein, it is preferable that the pH adjuster is phosphoric acid or asalt thereof.

When phosphoric acid or a salt thereof is used as the pH adjuster, ascompared with other inorganic acids or organic acids, preservationstability is further improved (period with preservation stability isfurther extended), and a change in a liquid property (pH) over timeduring preservation is suppressed.

In addition, it is preferable that the pH adjuster is sodiumdihydrogenphosphate or a mixture of sodium dihydrogenphosphate withdisodium hydrogenphosphate.

Moreover, by selecting sodium dihydrogenphosphate or the mixture ofsodium dihydrogenphosphate with disodium hydrogenphosphate, and bycombining this with sodium chlorite, an excessive progression of areaction in which sodium chlorite turns into chlorine dioxide hardlyoccurs. Therefore, a gas equilibration state is retained by replenishingchlorite ion from sodium chlorite that compensates only chlorine dioxidethat is lost by natural decomposition or that dissipates from a lidportion or walls of the container. As described above, the presentinvention is suitable in that unnecessary consumption of sodium chloriteis suppressed and sodium chlorite is efficiently consumed, leading tofurther improvement in preservation stability (period with preservationstability is further extended), and to further suppression of a changein chlorine dioxide concentration over time during preservation (boththe decrease and increase in the concentration can be suppressed). Inaddition, a mechanism of the chlorine dioxide solution containing thestabilizing composition of the present invention for replenishingchlorine dioxide from sodium chlorite for a long term is exerted even ina space or on a subject, to which the solution is applied, sprayed ordiffused. This provides an excellent sustained effect, i.e. lastingdisinfecting and deodorizing activity after application, spraying ordiffusion of the solution, further providing a great merit to the userupon its use.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a graph showing dissolved chlorine dioxide gas concentrationin a case where sodium dihydrogenphosphate was used in an amount of areaction equivalent or more and a case where citric acid was used in anamount of a reaction equivalent or more (the initial concentration was100 ppm)

FIG. 2 is a graph showing dissolved chlorine dioxide gas concentrationin a case where sodium dihydrogenphosphate was used in an amount of areaction equivalent or more and a case where citric acid was used in anamount of a reaction equivalent or more (the initial concentration was500 ppm).

BEST MODE FOR CARRYING OUT THE INVENTION

An embodiment of the present invention will be described below, but thepresent invention should not be limited to this embodiment.

(Chlorite)

For the chlorite to be used in the present invention, for example, saltsof alkali metal chlorite and salts of alkali earth metal chlorite can bementioned. Examples of the salt of alkali metal chlorite include sodiumchlorite, potassium chlorite and lithium chlorite. Examples of the saltof alkali earth metal chlorite include calcium chlorite, magnesiumchlorite and barium chlorite. Especially, not only from the viewpoint ofavailability, but also from the viewpoint of long-term preservationstability of the dissolved chlorine dioxide gas, sodium chlorite andpotassium chlorite are preferable, and sodium chlorite is mostpreferable.

(pH Adjuster)

For the pH adjuster to be used in the present invention, an acid(inorganic acid and organic acid) or a salt thereof, having a bufferingproprty whose pH is 2.5 to 6.8 as a 5% aqueous solution at 25° C., canbe mentioned. When the pH is below 2.5, or above 6.8, the preservationstability of the dissolved chlorine dioxide is reduced, and a change ina liquid property (pH) of the chlorine dioxide solution duringpreservation becomes large. It is preferable to use an acid (inorganicacid and organic acid) or a salt thereof having a buffering propertywhose pH is 3.5 to 6.0 as a 5% aqueous solution at 25° C., and it ismore preferable to use one having a pH of 4.0 to 5.5. Examples of theacid include phosphoric acid, boric acid, metaphosphoric acid,pyrophosphoric acid, sulfamic acid and acetic acid, and from theviewpoint of obtaining excellent preservation stability, inorganic acidor a salt thereof is preferred. Examples of the salt thereof includesodium dihydrogenphosphate and a mixture of sodium dihydrogenphosphatewith disodium hydrogenphosphate. Especially, phosphoric acid or a saltthereof is preferred, and sodium dihydrogenphosphate is more preferred,since preservation stability is excellent and a change in the liquidproperty (pH) during preservation is suppressed to a minimum, leading toexcellent disinfecting action, antiviral action, antifungal action,deodorizing action or the like. It should be noted that one kind of thepH adjuster may be used alone or two or more kinds thereof may be usedin combination. The final pure chlorine dioxide solution has a pH ofpreferably 4.5 to 6.5, more preferably 5.5 to 6.0, since preservationstability is excellent for a long term, and a pH change duringpreservation is suppressed.

(Preparative Example of Stabilizing Composition)

The stabilizing composition of the present invention including thechlorite and the pH adjuster (an acid or a salt thereof having abuffering property whose pH is 2.5 to 6.8 as a 5% aqueous solution at25° C.) may be, for example, obtained in the following manner.Specifically, a chlorite is dissolved in water to prepare 2,000 to180,000 ppm of an aqueous chlorite solution, and in the solution isdissolved a pH adjuster to prepare a stabilized solution. The amount ofthe pH adjuster is, for example, 0.5 to 100 g per 1,000 ml of theaqueous chlorite solution, with which the pH of the dissolved chlorinedioxide solution becomes 4.5 to 6.5, preferably 5.5 to 6.0.

(Preparative Example of Chlorine Dioxide Solution)

The chlorine dioxide solution may be, for example, obtained in thefollowing manner. Specifically, (a) a chlorite is dissolved in water toprepare 2,000 to 180,000 ppm of an aqueous solution of sodium chlorite,and (b) chlorine dioxide gas is bubbled and dissolved in water toprepare 100 to 2,900 ppm of an aqueous solution of chlorine dioxide.

Subsequently, 5.0 to 990 ml, preferably 50 to 300 ml of the aqueoussolution of chlorous acid (item (a)), 5.0 to 990 ml, preferably 50 to800 ml of the aqueous solution of chlorine dioxide (item (b)) and 5.0 to990 ml, preferably 50 to 400 ml of the stabilizing composition are mixedand stirred well at room temperature to thereby prepare a chlorinedioxide solution.

It is preferred that the final pH of the pure chlorine dioxide solutionis 4.5 to 6.5. When the pH is out of this range, the preservationstability is reduced, which may lead to, for example, fluctuation of thepharmacological activity during preservation, and to attenuation in thepharmacological activity after long-term (e.g. 2-year) preservation. Inthe present invention, more preferable pH range of the pure chlorinedioxide solution is 5.5 to 6.0.

EXAMPLE 1

In the following manner, a chlorine dioxide solution was prepared.Specifically, to 250 ml of water in which 2,000 ppm of chlorine dioxidegas had been dissolved were added 680 ml of water and then 80 ml of a25% solution of sodium chlorite, and stirred. Subsequently, to thesolution was added sodium dihydrogenphosphate (having a pH of 4.1 to 4.5as a 5% aqueous solution at 25° C.) in such an amount that the pH of thesolution became 5.5 to 6.0 and stirred, to thereby obtain 1,000 ml of achlorine dioxide solution including: a chlorine dioxide gas dissolvedtherein; and a stabilizing composition including sodium chlorite andsodium dihydrogenphosphate.

COMPARATIVE EXAMPLE 1

A chlorine dioxide solution as a control was prepared in the same manneras in Example 1, except that citric acid (having a pH of 1.8 to 2.2 as a5% aqueous solution at 25° C.) was used instead of sodiumdihydrogenphosphate.

(Stabilizing Test)

The chlorine dioxide solution obtained in Example 1 was diluted by aconventional method, to thereby prepare chlorine dioxide solutionshaving concentrations of 100 ppm and 500 ppm. Likewise, the chlorinedioxide solution obtained in Comparative Example 1 was used to therebyprepare solutions having chlorine dioxide concentrations of 100 ppm and500 ppm.

In order to determine the preservation stability of these solutions,changes in the chlorine dioxide concentration (ppm) and in the liquidproperty (pH) over time were measured. For the stabilizing test, anaccelerated aging test (measurement temperature: 54° C., 14 dayscorrespond to one year at normal temperature) was performed inaccordance with a conventional method. The results of the preservationstability are shown in Tables below and the drawings (comparative datais shown between a case where sodium dihydrogenphosphate was used in anamount of a reaction equivalent or more and a case where citric acid wasused in an amount of a reaction equivalent or more).

TABLE 1 (Concentration: 100 ppm, sodium (Concentration: 100 ppm,dihydrogenphosphate was used) citric acid was used) Dissolved DissolvedClO₂ (ppm) ClO₂ (ppm) Start 116 Start 121  1 day later 143  1 day later1,551  5 days later 154  5 days later 935 10 days later 149 10 dayslater 269 15 days later 128 15 days later 69 20 days later 128 20 dayslater — 25 days later 129 25 days later — *54° C.-accelerated aging test(14 days correspond to one year at normal temperature)

TABLE 2 (Concentration: 500 ppm, sodium (Concentration: 500 ppm,dihydrogenphosphate was used) citric acid was used) Dissolved DissolvedClO₂ (ppm) ClO₂ (ppm) Start 523 Start 567  1 day later 554  1 day later3,474  5 days later 546  5 days later 1,160 10 days later 532 10 dayslater 286 15 days later 538 15 days later 150 20 days later 516 20 dayslater — 25 days later 476 25 days later — *54° C.-accelerated aging test(14 days correspond to one year at normal temperature)

As is apparent from the above-described tables and accompanied drawings,the pH adjuster whose pH is 2.5 to 6.8 as a 5% aqueous solution at 25°C. remarkably enhances the preservation stability of the chlorinedioxide solution, and suppresses a change in the liquid property (pH)during preservation, as compared with an acid having a bufferingproperty whose pH is outside the range of from 2.5 to 6.8. Accordingly,for example, when dissolved chlorine dioxide is used in disinfectant,deodorant, antifungal agent or the like, the stabilizing composition ofthe present invention can provide highly reliable products to themarket.

INDUSTRIAL APPLICABILITY

The stabilizing composition according to the present invention issuitably utilized in an agent containing chlorine dioxide, such asdisinfectant, deodorant and fungicide, in order to hold the chlorinedioxide concentration in an approximately constant range for a longterm.

1. A composition for stabilizing chlorine dioxide, which maintains achlorine dioxide concentration nearly constant in an agent comprisingchlorine dioxide dissolved therein even when chlorine dioxide iscontinuously released as gas from the agent, comprising: a chlorite anda pH adjuster which is an acid or a salt thereof having a bufferingproperty whose pH is 2.5 to 6.8 as a 5% aqueous solution at 25° C. 2.The composition for stabilizing chlorine dioxide according to claim 1,wherein the pH adjuster is phosphoric acid or a salt thereof.
 3. Thecomposition for stabilizing chlorine dioxide according to claim 2,wherein the pH adjuster is one of sodium dihydrogenphosphate and amixture of sodium dihydrogenphosphate with disodium hydrogenphosphate.